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Oxidative Medicine and Cellular Longevity
|
March 29, 2017
BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage
Li-Xia Qin, Jie-Qiong Tan, Hai-Nan Zhang, et al.
Plant Physiology and Biochemistry : PPB
|
March 19, 2025
Identification of stay-green candidate gene TaTRNH1-3B and development of molecular markers related to chlorophyll content and yield in wheat (Triticum aestivum L.)
Xiu-Juan Jin, Xue Yan, Feng Guo, et al.
Asian Journal of Andrology
|
February 1, 2022
The comparison of survival between active surveillance or watchful waiting and focal laser ablation in patients with low-risk prostate cancer
Jia-Kun Li, Chi-Chen Zhang, Shi Qiu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 11, 2005
[Detection of duplications or deletions of the PMP22 gene using real-time quantitative PCR]
Fu-feng Zhang, Bei-sha Tang, Yan Shen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 13, 2009
Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings
Jun-Ling Wang, Bin Xiao, Xiang-Xiang Cui, et al.
Neurobiology of Aging
|
October 12, 2021
Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease
Li Jiang, Jun-Pu Mei, Yu-Wen Zhao, et al.
European Journal of Medical Genetics
|
May 14, 2013
Exome sequencing released a case of X-linked adrenoleukodystrophy mimicking recessive hereditary spastic paraplegia
Zi-Xiong Zhan, Xin-Xin Liao, Juan Du, et al.
Neurobiology of Aging
|
April 30, 2022
PSEN1 G417S mutation in a Chinese pedigree causing early-onset parkinsonism with cognitive impairment
Li Jiang, Yan Qin, Yu-Wen Zhao, et al.
Neuroscience Letters
|
December 22, 2014
Analysis of several loci from genome-wide association studies in Parkinson's disease in mainland China
Zhen-Hua Liu, Ji-Feng Guo, Kai Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 22, 2019
A retrospective review of multiple findings in diagnostic exome sequencing: half are distinct and half are overlapping diagnoses
Erica D Smith, Kirsten Blanco, Samin A Sajan, et al.
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Search research articles
Search
Showing results (341-350 of 449) with videos related to
Sort By:
Page
of 45
Oxidative Medicine and Cellular Longevity
|
March 29, 2017
BAG5 Interacts with DJ-1 and Inhibits the Neuroprotective Effects of DJ-1 to Combat Mitochondrial Oxidative Damage
Li-Xia Qin, Jie-Qiong Tan, Hai-Nan Zhang, et al.
Plant Physiology and Biochemistry : PPB
|
March 19, 2025
Identification of stay-green candidate gene TaTRNH1-3B and development of molecular markers related to chlorophyll content and yield in wheat (Triticum aestivum L.)
Xiu-Juan Jin, Xue Yan, Feng Guo, et al.
Asian Journal of Andrology
|
February 1, 2022
The comparison of survival between active surveillance or watchful waiting and focal laser ablation in patients with low-risk prostate cancer
Jia-Kun Li, Chi-Chen Zhang, Shi Qiu, et al.
Zhonghua Yi Xue Yi Chuan Xue Za Zhi = Zhonghua Yixue Yichuanxue Zazhi = Chinese Journal of Medical Genetics
|
October 11, 2005
[Detection of duplications or deletions of the PMP22 gene using real-time quantitative PCR]
Fu-feng Zhang, Bei-sha Tang, Yan Shen, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 13, 2009
Analysis of SCA2 and SCA3/MJD repeats in Parkinson's disease in mainland China: genetic, clinical, and positron emission tomography findings
Jun-Ling Wang, Bin Xiao, Xiang-Xiang Cui, et al.
Neurobiology of Aging
|
October 12, 2021
Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease
Li Jiang, Jun-Pu Mei, Yu-Wen Zhao, et al.
European Journal of Medical Genetics
|
May 14, 2013
Exome sequencing released a case of X-linked adrenoleukodystrophy mimicking recessive hereditary spastic paraplegia
Zi-Xiong Zhan, Xin-Xin Liao, Juan Du, et al.
Neurobiology of Aging
|
April 30, 2022
PSEN1 G417S mutation in a Chinese pedigree causing early-onset parkinsonism with cognitive impairment
Li Jiang, Yan Qin, Yu-Wen Zhao, et al.
Neuroscience Letters
|
December 22, 2014
Analysis of several loci from genome-wide association studies in Parkinson's disease in mainland China
Zhen-Hua Liu, Ji-Feng Guo, Kai Li, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics
|
March 22, 2019
A retrospective review of multiple findings in diagnostic exome sequencing: half are distinct and half are overlapping diagnoses
Erica D Smith, Kirsten Blanco, Samin A Sajan, et al.
Page
of 45